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Ligand 4-nitrophenyl 5-O-(E)-feruloyl-alpha-L-arabinofuranoside

Basic Ligand Information

Molecular Structure

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Roles as Enzyme Ligand

Substrate in Enzyme-catalyzed Reactions (5 results)

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Show Substrate (5 entries)

EC NUMBER

REACTION

REACTION DIAGRAM

LITERATURE

ENZYME 3D STRUCTURE

3.1.1.73

4-nitrophenyl 5-O-(E)-feruloyl-alpha-L-arabinofuranoside + H2O = 4-nitrophenyl alpha-L-arabinofuranoside + ferulate

680967

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3.1.1.73

4-nitrophenyl 5-O-(E)-feruloyl-alpha-L-arabinofuranoside + H2O = 4-nitrophenyl-alpha-L-arabinofuranoside + ferulate

680967

-

3.1.1.73

4-nitrophenyl 5-O-(E)-feruloyl-alpha-L-arabinofuranoside + H2O = 4-nitrophenyl-alpha-L-arabinofuranoside + trans-ferulate

680967

-

3.1.1.73

4-nitrophenyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside + H2O = 4-nitrophenyl-alpha-L-arabinofuranoside + trans-ferulate

682613

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3.1.1.73

4-nitrophenyl 5-O-trans-feruloyl-alpha-L-arabinofuranoside + H2O = ferulic acid + 4-nitrophenyl alpha-L-arabinofuranoside

667243, 668435, 668444, 667181, 695792

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3.1.1.73

5 entries

Enzyme Kinetic Parameters

k_cat Value (Turnover Number) (8 results)

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Show Turnover Number (8 entries)

EC NUMBER

TURNOVER NUMBER [1/S]

TURNOVER NUMBER MAXIMUM [1/S]

COMMENTARY

LITERATURE

3.1.1.73

1.55

-

-

695792

3.1.1.73

2.73

-

-

680967

3.1.1.73

3.66

-

-

680967

3.1.1.73

10.3

-

-

668444

3.1.1.73

22.5

-

-

680967

3.1.1.73

65.5

-

30°C

667243

3.1.1.73

166.7

-

pH 6.0, 45°C

668435

3.1.1.73

175

-

-

680967

3.1.1.73

8 entries

K_M Value (9 results)

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Show KM Value (9 entries)

EC NUMBER

KM VALUE [MM]

KM VALUE MAXIMUM [MM]

COMMENTARY

LITERATURE

3.1.1.73

0.016

-

-

680967

3.1.1.73

0.073

-

-

680967

3.1.1.73

0.123

-

-

680967

3.1.1.73

0.23

-

pH 5.5, 30°C

667181

3.1.1.73

0.27

-

30°C

667243

3.1.1.73

0.28

-

-

680967

3.1.1.73

0.57

-

-

668444

3.1.1.73

1.6

-

pH 6.0, 45°C

668435

3.1.1.73

3332

-

-

695792

3.1.1.73

9 entries

References & Links

Literature References (7)

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Show Reference (7 entries)

BRENDA REFERENCE ID

PUBMED ID

TITLE

YEAR

AUTHORS

JOURNAL

VOLUME

PAGES

667181

12441154

Differentiation of feruloyl esterases on synthetic substrates in alpha-arabinofuranosidase-coupled and ultraviolet-spectrophotometric assays

2002

Biely, P.; Mastihubova, M.; van Zyl, W.H.; Prior, B.A.

Anal. Biochem.

311

68-75

667243

12957952

Purification and properties of a feruloyl esterase involved in lignocellulose degradation by Aureobasidium pullulans

2003

Rumbold, K.; Biely, P.; Mastihubova, M.; Gudelj, M.; Gubitz, G.; Robra, K.H.; Prior, B.A.

Appl. Environ. Microbiol.

69

5622-5626

668435

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Purification and characterization of a Fusarium oxysporum feruloyl esterase (FoFAE-I) catalysing transesterification of phenolic acid esters

2003

Topakas, E.; Stamatis, H.; Mastihubova, M.; Biely, P.; Kekos, D.; Macris, B.J.; Christakopoulos, P.

Enzyme Microb. Technol.

33

729-737

668444

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Sporotrichum thermophile type C feruloyl esterase (StFaeC): purification, characterization, and its use for phenolic acid (sugar) ester synthesis

2005

Topakas, E.; Vafiadi, C.; Stamatis, H.; Christakopoulos, P.

Enzyme Microb. Technol.

36

729-736

680967

16901567

Substrate and positional specificity of feruloyl esterases for monoferuloylated and monoacetylated 4-nitrophenyl glycosides

2007

Puchart, V.; Vrsanska, M.; Mastihubova, M.; Topakas, E.; Vafiadi, C.; Faulds, C.B.; Tenkanen, M.; Christakopoulos, P.; Biely, P.

J. Biotechnol.

127

235-243

682613

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Microbial production, characterization and applications of feruloyl esterases

2007

Topakas, E.; Vafiadi, C.; Christakopoulos, P.

Process Biochem.

42

497-509

695792

18414848

Cloning, characterization and functional expression of an alkalitolerant type C feruloyl esterase from Fusarium oxysporum

2008

Moukouli, M.; Topakas, E.; Christakopoulos, P.

Appl. Microbiol. Biotechnol.

79

245-254

Links to other databases for 4-nitrophenyl 5-O-(E)-feruloyl-alpha-L-arabinofuranoside

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Show Links (1 entry)

ChEBI

PubChem

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